Cost-Effectiveness Analysis of Contemporary Advanced Prostate Cancer Treatment Sequences
- PMID: 40277797
- PMCID: PMC12025438
- DOI: 10.3390/curroncol32040240
Cost-Effectiveness Analysis of Contemporary Advanced Prostate Cancer Treatment Sequences
Abstract
There has been a proliferation of novel treatments for the management of advanced prostate cancer (PCa), including androgen receptor pathway inhibitors (ARPI). Although there are health economic analyses of novel PCa treatments, such as ARPIs for specific health states, there is a lack of sequential analyses. Our paper aims to fill this gap. We developed a Monte Carlo Markov model to simulate the management of advanced PCa to end-of-life. We modeled patients who begin in metastatic and nonmetastatic castration-sensitive PCa (mCSPC and nmCSPC), with risk stratification for mCSPC, progressing to metastatic castration-resistant PCa (mCRPC). Using current guidelines and recent literature, we simulated admissible treatment sequences over these states along a 15-year horizon. We report the best treatment sequences in terms of efficacy and cost-effectiveness. We find that the most cost-effective use of ARPIs is early in advanced PCa for a cost-effectiveness threshold (CET) of CAD 100K per QALY. For a CET of CAD 50K per QALY, early ARPI use is most cost-effective in mCSPC-starting patients but not nmCSPC-starting. We conclude that the most cost-effective way to use ARPIs is when patients first enter advanced PCa. The most cost-effective ARPI at current Canadian prices is abiraterone, mostly due to abiraterone's lower price level.
Keywords: androgen-receptor pathway inhibitor; cost-effectiveness; prostate cancer; treatment sequence.
Conflict of interest statement
The authors declare no conflicts of interest.
Figures



Similar articles
-
Cost Effectiveness of Systemic Treatment Intensification for Metastatic Hormone-sensitive Prostate Cancer: Is Triplet Therapy Cost Effective?Eur Urol Oncol. 2024 Aug;7(4):870-876. doi: 10.1016/j.euo.2023.11.013. Epub 2023 Dec 6. Eur Urol Oncol. 2024. PMID: 38057191
-
A Real World Observational Study Characterizing Patients With Advanced Prostate Cancer Treated With or Without Androgen Receptor-Pathway-Inhibitor Therapies in Alberta, Canada.Clin Genitourin Cancer. 2024 Oct;22(5):102115. doi: 10.1016/j.clgc.2024.102115. Epub 2024 May 9. Clin Genitourin Cancer. 2024. PMID: 38890099
-
Real-world prevalence of adverse events with first-line systemic therapies among patients with metastatic castration-sensitive prostate cancer.Prostate. 2024 Nov;84(15):1387-1397. doi: 10.1002/pros.24777. Epub 2024 Aug 20. Prostate. 2024. PMID: 39162127
-
Current Systemic Therapy in Men with Metastatic Castration-Sensitive Prostate Cancer.Curr Oncol Rep. 2024 May;26(5):488-495. doi: 10.1007/s11912-024-01509-6. Epub 2024 Apr 9. Curr Oncol Rep. 2024. PMID: 38592590 Review.
-
Cost-effectiveness analyses and cost analyses in castration-resistant prostate cancer: A systematic review.PLoS One. 2018 Dec 5;13(12):e0208063. doi: 10.1371/journal.pone.0208063. eCollection 2018. PLoS One. 2018. PMID: 30517165 Free PMC article.
References
-
- Freedland S.J., Luz M.d.A., De Giorgi U., Gleave M., Gotto G.T., Pieczonka C.M., Haas G.P., Kim C.-S., Ramirez-Backhaus M., Rannikko A., et al. Improved Outcomes with Enzalutamide in Biochemically Recurrent Prostate Cancer. N. Engl. J. Med. 2023;389:1453–1465. doi: 10.1056/NEJMoa2303974. - DOI - PubMed
-
- Chi K.N., Chowdhury S., Bjartell A., Chung B.H., Pereira de Santana Gomes A.J., Given A., Juárez A., Merseburger A.S., Özgüroğlu M., Uemura H., et al. Apalutamide in patients with metastatic castration-sensitive prostate cancer: Final survival analysis of the randomized, double-blind, phase III TITAN study. J. Clin. Oncol. 2021;39:2294–2303. doi: 10.1200/JCO.20.03488. - DOI - PubMed
-
- Fizazi K., Foulon S., Carles J., Roubaud G., McDermott R., Fléchon A., Tombal B., Supiot S., Berthold D., Ronchin P., et al. Abiraterone plus prednisone added to androgen deprivation therapy and docetaxel in de novo metastatic castration-sensitive prostate cancer (PEACE-1): A multicentre, open-label, randomised, phase 3 study with a 2×2 factorial design. Lancet. 2022;399:1695–1707. doi: 10.1016/S0140-6736(22)00367-1. - DOI - PubMed
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous